Eligibility Criteria

Inclusion and exclusion criteria
Descrizione

Inclusion and exclusion criteria

1. Previously untreated, diagnoses of Chronic Lymphocytic Leukemia with paired normal DNA (Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation). 2. Matched,clonally related Chronic Lymphocytic Leukemia and Richter Syndrome cases (Genetic Lesions associated with Chronic Lymphocytic Leukemia transformation to Richter Syndrome).
Descrizione

1. Previously untreated, diagnoses of Chronic Lymphocytic Leukemia with paired normal DNA (Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation). 2. Matched,clonally related Chronic Lymphocytic Leukemia and Richter Syndrome cases (Genetic Lesions associated with Chronic Lymphocytic Leukemia transformation to Richter Syndrome).

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0332155
UMLS CUI [1,2]
C0023434
UMLS CUI [2,1]
C0023434
UMLS CUI [2,2]
C0349631

Similar models

Eligibility Criteria

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion and exclusion criteria
1. Previously untreated, diagnoses of Chronic Lymphocytic Leukemia with paired normal DNA (Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation). 2. Matched,clonally related Chronic Lymphocytic Leukemia and Richter Syndrome cases (Genetic Lesions associated with Chronic Lymphocytic Leukemia transformation to Richter Syndrome).
Item
1. Previously untreated, diagnoses of Chronic Lymphocytic Leukemia with paired normal DNA (Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation). 2. Matched,clonally related Chronic Lymphocytic Leukemia and Richter Syndrome cases (Genetic Lesions associated with Chronic Lymphocytic Leukemia transformation to Richter Syndrome).
boolean
C0332155 (UMLS CUI [1,1])
C0023434 (UMLS CUI [1,2])
C0023434 (UMLS CUI [2,1])
C0349631 (UMLS CUI [2,2])